Cas 119447-89-1,(2R,3S,4R)-3,4-Bis-benzyloxy-2-((2R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-6,8-dioxa-bicyclo[3.2.1]octane

119447-89-1

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Basic information

Product Name: (2R,3S,4R)-3,4-Bis-benzyloxy-2-((2R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-6,8-dioxa-bicyclo[3.2.1]octane
Synonyms:
CAS NO:119447-89-1
Molecular Formula:
Molecular Weight: 758.909
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2R,3S,4R)-3,4-Bis-benzyloxy-2-((2R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-6,8-dioxa-bicyclo[3.2.1]octane(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S,4R)-3,4-Bis-benzyloxy-2-((2R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-6,8-dioxa-bicyclo[3.2.1]octane(119447-89-1)
EPA Substance Registry System: (2R,3S,4R)-3,4-Bis-benzyloxy-2-((2R,4R,5S,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-6,8-dioxa-bicyclo[3.2.1]octane(119447-89-1)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 119447-89-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119447-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,4,4 and 7 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 119447-89:
(8*1)+(7*1)+(6*9)+(5*4)+(4*4)+(3*7)+(2*8)+(1*9)=151
151 % 10 = 1
So 119447-89-1 is a valid CAS Registry Number.

119447-89-1Upstream product

119447-85-7 (2R,3S,4R)-3,4-Bis-benzyloxy-2-((3R,4S,5R,6R)-4,5-bis-benzyloxy-6-benzyloxymethyl-3-phenylsulfanyl-tetrahydro-pyran-2-yloxy)-6,8-dioxa-bicyclo[3.2.1]octane

119447-89-1Downstream Products

119447-89-1Relevant academic research and scientific papers

A Convenient Synthesis of 2-Deoxy-β-D-glucopyranosides

Preuss, Rainer,Schmidt, Richard R.

, p. 694 - 697 (1988)

The O-(2-deoxy-2-phenylthio-α-D-glucopyranosyl) trichloroacetimidate α-3 was obtained from 3,4,6-tri-O-benzyl-D-glucal (1) in a two-step procedure.This compound is a powerful glucopyranosyl donor, which with typical alcohol acceptors provided mainly the c

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